Related gene-specific medical variations for Gene (Select 1780) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3086444	NM_001135556.2(DYNC1I1):c.1879T>C (p.Ser627Pro)	DYNC1I1, LOC110121293 (S644P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3001288	NM_001135556.2(DYNC1I1):c.1793A>G (p.Asn598Ser)	DYNC1I1, LOC110121293 (N595S +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2975551	NM_001135556.2(DYNC1I1):c.1854C>T (p.Ser618=)	DYNC1I1, LOC110121293	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1624070	NM_001135556.2(DYNC1I1):c.1596C>T (p.Ala532=)	DYNC1I1, LOC110121292	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1545765	NM_001135556.2(DYNC1I1):c.1638C>T (p.Asn546=)	LOC110121292, DYNC1I1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1270005	NM_001135556.2(DYNC1I1):c.*109T>C	DYNC1I1, LOC110121293	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign

ClinVar